1mh1

Disease
Known disease associated with this structure: Night blindness, congenital stationery, rhodopsin-related OMIM:[180380], Retinitis pigmentosa, autosomal recessive OMIM:[180380], Retinitis pigmentosa-4, autosomal dominant OMIM:[180380]

About this Structure
1MH1 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference
Page seeded by OCA on Tue Feb 17 14:16:50 2009